Canonical Allele Identifier: PA2827315701
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 195130
ClinVar RCV Id: RCV001035816 RCV000656993 RCV000765689 RCV002252019 RCV002426841
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317023.1:p.Gln90His
CA241414
NM_001330094.2:c.270G>T
CA346824342
NM_001330094.2:c.270G>C